hm1

Slc45a2^Uw-dbr/Slc45a2^Uw-dbr
B10.PL-H2^u/(73NS)Sn

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	Euro	Europhenome
N	normal phenotype

pigmentation

irregular coat pigmentation ( J:41299 )

• light beige; reduced pigmentation, more severe than in heterozygotes

integument

irregular coat pigmentation ( J:41299 )

• light beige; reduced pigmentation, more severe than in heterozygotes

Mouse Models of Human Disease		OMIM ID	Ref(s)
Albinism, Oculocutaneous, Type IV; OCA4		606574	J:41299

ht2

Slc45a2^Uw-dbr/Slc45a2⁺
B10.PL-H2^u/(73NS)Sn

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	Euro	Europhenome
N	normal phenotype

pigmentation

irregular coat pigmentation ( J:41299 )

• dark brown; reduced pigmentation, less severe than in homozygotes

integument

irregular coat pigmentation ( J:41299 )

• dark brown; reduced pigmentation, less severe than in homozygotes

Mouse Models of Human Disease		OMIM ID	Ref(s)
Albinism, Oculocutaneous, Type IV; OCA4		606574	J:41299